Preterm Labor Clinical Trial
Official title:
Adjunctive Vaginal Progesterone (Micronized Progesterone Effervescent Vaginal Tablet) in Management of Preterm Labor: A Randomized Controlled Trial
This study evaluates the addition of vaginal micronized progesterone effervescent to standard treatment in the treatment of preterm labor. Half of participants will receive vaginal micronized progesterone effervescent and standard treatment, while the other half will receive only standard treatment.
Status | Recruiting |
Enrollment | 48 |
Est. completion date | October 31, 2025 |
Est. primary completion date | August 31, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - singleton pregnancy with gestational age 24-33 weeks 6 days - preterm labor - received treatment with tocolysis and corticosteroids Exclusion Criteria: - conditions that need immediate delivery such as fetal distress, chorioamnionitis - have medical complications such as heart disease, seizure - fetal anomalies - cervical dilatation more than 5 cm - allergy to progesterone - contraindication to progesterone - contraindication to tocolytic use |
Country | Name | City | State |
---|---|---|---|
Thailand | Vorapong Phupong | Bangkok |
Lead Sponsor | Collaborator |
---|---|
Chulalongkorn University |
Thailand,
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American College of Obstetricians and Gynecologists' Committee on Practice Bulletins-Obstetrics. Practice Bulletin No. 171: Management of Preterm Labor. Obstet Gynecol. 2016 Oct;128(4):e155-64. doi: 10.1097/AOG.0000000000001711. — View Citation
Ashoush S, El-Kady O, Al-Hawwary G, Othman A. The value of oral micronized progesterone in the prevention of recurrent spontaneous preterm birth: a randomized controlled trial. Acta Obstet Gynecol Scand. 2017 Dec;96(12):1460-1466. doi: 10.1111/aogs.13236. — View Citation
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Martinez de Tejada B, Karolinski A. Vaginal progesterone for maintenance tocolysis: a systematic review and metaanalysis of randomized trials. Am J Obstet Gynecol. 2015 Sep;213(3):438-9. doi: 10.1016/j.ajog.2015.05.037. Epub 2015 May 21. No abstract avail — View Citation
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | latency period | time from preterm labor to delivery | 13 weeks | |
Secondary | gestational age at delivery | mean gestational age at delivery | 13 weeks | |
Secondary | preterm delivery less than 34 weeks | percentage of preterm delivery less than 34 weeks | 10 weeks | |
Secondary | preterm delivery less than 37 weeks | percentage of preterm delivery less than 37 weeks | 13 weeks | |
Secondary | neonatal complications | percentage of newborn with RDS, IVH, NEC, death | 13 weeks | |
Secondary | side effects | percentage of side effects such as headache, nausea/vomiting | 13 weeks | |
Secondary | compliance | percentage of complete drug use | 13 weeks | |
Secondary | good satisfaction | percentage of good satisfaction | 13 weeks | |
Secondary | good quality of life | percentage of good quality of life | 13 weeks | |
Secondary | Time to the recurrence of uterine contractions | mean time to the recurrence of uterine contractions | 13 weeks |
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